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  1. Bernal, Louis Carlos [Photographer]; Ferrer, Elizabeth [Author] ; Senf, Rebecca A. [Writer of supplementary textual content]

    Louis Carlos Bernal : monografía - [First edition]

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    New York, NY: Aperture, 2024 ; Tuscon, AZ: Center for Creative Photography, 2024

  2. Avedon, Richard [Photographer] ; Senf, Rebecca A. [Editor] Civico Museo d'Arte Contemporanea

    Richard Avedon, relationships

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    Milano: Skira, 2022

  3. Smith, Rodney [Photographer] ; Martineau, Paul [Writer of supplementary textual content]; Carter, Graydon [Writer of supplementary textual content]; Senf, Rebecca A. [Writer of supplementary textual content] J. Paul Getty Museum

    Rodney Smith : a leap of faith

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    Los Angeles: J. Paul Getty Museum, [2023]

  5. Marc, Stephen [Photographer]; Senf, Rebecca A. [Interviewer] ; Kouwenhoven, Bill [Writer of introduction]

    American true colors

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    Staunton, Virginia: George F. Thompson Publishing, 2020

  7. Schüle, Rebecca; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; Baets, Jonathan; Balicza, Peter; Chinnery, Patrick; Dürr, Alexandra; Haack, Tobias; Hengel, Holger; Horvath, Rita; Houlden, Henry; Kamsteeg, Erik-Jan; Kamsteeg, Christoph; Lohmann, Katja; Macaya, Alfons; Marcé-Grau, Anna; Maver, Ales; Molnar, Judit; Münchau, Alexander; Peterlin, Borut; Riess, Olaf; Schöls, Ludger; [...]

    Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint

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    Springer Science and Business Media LLC, 2021

    Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1462-1465

  8. Schüle, Rebecca; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; Baets, Jonathan; Balicza, Peter; Chinnery, Patrick; Dürr, Alexandra; Haack, Tobias; Hengel, Holger; Horvath, Rita; Houlden, Henry; Kamsteeg, Erik-Jan; Kamsteeg, Christoph; Lohmann, Katja; Macaya, Alfons; Marcé-Grau, Anna; Maver, Ales; Molnar, Judit; Münchau, Alexander; Peterlin, Borut; Riess, Olaf; Schöls, Ludger; [...]

    Solving unsolved rare neurological diseases—a Solve-RD viewpoint

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    Springer Science and Business Media LLC, 2021

    Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1332-1336

  9. Zurek, Birte; Ellwanger, Kornelia; Vissers, Lisenka E. L. M.; Schüle, Rebecca; Synofzik, Matthis; Töpf, Ana; de Voer, Richarda M.; Laurie, Steven; Matalonga, Leslie; Gilissen, Christian; Ossowski, Stephan; ’t Hoen, Peter A. C.; Vitobello, Antonio; Schulze-Hentrich, Julia M.; Riess, Olaf; Brunner, Han G.; Brookes, Anthony J.; Rath, Ana; Bonne, Gisèle; Gumus, Gulcin; Verloes, Alain; Hoogerbrugge, Nicoline; Evangelista, Teresinha; Harmuth, Tina; [...]

    Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

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    Springer Science and Business Media LLC, 2021

    Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1459-1461

  10. Zurek, Birte; Ellwanger, Kornelia; Vissers, Lisenka E. L. M.; Schüle, Rebecca; Synofzik, Matthis; Töpf, Ana; de Voer, Richarda M.; Laurie, Steven; Matalonga, Leslie; Gilissen, Christian; Ossowski, Stephan; ’t Hoen, Peter A. C.; Vitobello, Antonio; Schulze-Hentrich, Julia M.; Riess, Olaf; Brunner, Han G.; Brookes, Anthony J.; Rath, Ana; Bonne, Gisèle; Gumus, Gulcin; Verloes, Alain; Hoogerbrugge, Nicoline; Evangelista, Teresinha; Harmuth, Tina; [...]

    Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

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    Springer Science and Business Media LLC, 2021

    Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1325-1331

  11. Matalonga, Leslie; Hernández-Ferrer, Carles; Piscia, Davide; Cohen, Enzo; Cuesta, Isabel; Danis, Daniel; Denommé-Pichon, Anne-Sophie; Duffourd, Yannis; Gilissen, Christian; Johari, Mridul; Laurie, Steven; Li, Shuang; Matalonga, Leslie; Nelson, Isabelle; Peters, Sophia; Paramonov, Ida; Prasanth, Sivakumar; Robinson, Peter; Sablauskas, Karolis; Savarese, Marco; Steyaert, Wouter; van der Velde, Joeri K.; Vitobello, Antonio; Schüle, Rebecca; [...]

    Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

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    Springer Science and Business Media LLC, 2021

    Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1466-1469

  12. Matalonga, Leslie; Hernández-Ferrer, Carles; Piscia, Davide; Cohen, Enzo; Cuesta, Isabel; Danis, Daniel; Denommé-Pichon, Anne-Sophie; Duffourd, Yannis; Gilissen, Christian; Johari, Mridul; Laurie, Steven; Li, Shuang; Matalonga, Leslie; Nelson, Isabelle; Peters, Sophia; Paramonov, Ida; Prasanth, Sivakumar; Robinson, Peter; Sablauskas, Karolis; Savarese, Marco; Steyaert, Wouter; van der Velde, Joeri K.; Vitobello, Antonio; Schüle, Rebecca; [...]

    Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

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    Springer Science and Business Media LLC, 2021

    Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1337-1347

  13. Jackson, Adam; Lin, Sheng-Jia; Jones, Elizabeth A.; Chandler, Kate E.; Orr, David; Moss, Celia; Haider, Zahra; Ryan, Gavin; Holden, Simon; Harrison, Mike; Burrows, Nigel; Jones, Wendy D.; Loveless, Mary; Petree, Cassidy; Stewart, Helen; Low, Karen; Donnelly, Deirdre; Lovell, Simon; Drosou, Konstantina; Ambrose, J.C.; Arumugam, P.; Bevers, R.; Bleda, M.; Boardman-Pretty, F.; [...]

    Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

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    Elsevier BV, 2023

    Published in: Human Genetics and Genomics Advances, 4 (2023) 2, Seite 100186